[0001] This invention relates to a class of penicillanic acid derivatives which are useful
as β-lactamase inhibitors.
[0002] Certain 6β-sulphonyloxypenicillanic acids are known [Sheehan et al. Cambridge symposium
on β-lactam antibiotics June 1976; and USP 4143046]. However in the past these compounds
have only been disclosed as having antibacterial activity, which has proved disappointing.
No mention has been made that any of these compounds might possess β-lactamase inhibitory
properties. Surprisingly, it has been found that these and related compounds possess
the ability to enhance the effectiveness of penicillins and cephalosporins.
[0003] The present invention provides a pharmaceutical composition comprising:
(a) a pharmaceutically acceptable carrier;
(b) a compound of the formula (I):
and pharmaceutically acceptable salts and in vivo hydrolysable esters thereof, wherein
n is O or 2, R1 is a Cl-6 alkyl group optionally substituted with one, two or three fluorine, chlorine or bromine
atoms, or is a di-Cl-6 alkylamino group or is a group of the formula (i):
wherein X is a bond, or a -CH=CH group, or a methylene or ethylene group; R2 is a hydrogen, fluorine, bromine or chlorine atom, or is an amino, protected amino,
hydroxy, protected hydroxy, C1-6 alkyl, nitro, di-C1-6 alkylamino, acetamido, C1-6 alkoxy or trifluromethyl group; R3 is a hydrogen or chlorine atom or a C1-6 alkyl or trifluoromethyl group; and R4 is a hydrogen or chlorine atom, or a C1-6 alkyl or C1-6 alkoxy group; or R2 and R3 on any two adjacent carbon atoms may together represent a buta-l,3-dienylene moiety
which is optionally substituted by a C1-3 alkyl or C1-3 alkoxy group; and
(c) a penicillin or cephalosporin or a pharmaceutically acceptable salt or in vivo
hydrolysable ester thereof.
[0004] When the terms "protected amino" and "protected hydroxy" are used in this specification,
the groups used herein for protecting these functions are those that may be removed
when desired; for example any of such group known in the art, such as a benzyloxycarbonyl,
p-nitrobenzyloxycarbonyl or benzyl group.
[0005] Preferably n is zero.
[0006] Suitably R
1 is a C
1-6 alkyl group optionally substituted with one, two or three fluorine, chlorine or bromine
atoms.
[0007] More suitably R
1 is a methyl, ethyl, propyl, chloropropyl or isopropyl group.
[0008] In compounds of the formula (i) suitably X is a bond or a methylene group.
[0009] Apt values for R
2 include the hydrogen, fluorine, chlorine and bromine atoms, and amino, protected
amino, hydroxy, protected hydroxy, C
1-5 alkyl, nitro, C
1-6 alkylamino, acetamido, C
1-6 alkoxy and trifluoromethyl groups.
[0010] Suitably R
2 is a hydrogen, fluorine, bromine or chlorine atom, or a methyl or methoxy group.
[0011] A preferred value of R
2 is methyl.
[0012] A further preferred value of R
2 is bromine.
[0013] Apt values for R are a hydrogen or chlorine atom, or a C
1-6 alkyl or trifluoromethyl group.
[0014] Suitably R
3 is a hydrogen or chlorine atom.
[0015] A preferred value for R
3 is hydrogen.
[0016] Apt values for R are a hydrogen or chlorine atom, or a C
l-6 alkyl group.
[0017] Suitably R
4 is a hydrogen or chlorine atom.
[0018] A preferred value for R
4 is hydrogen.
[0019] Thus it is to be realised that a particularly suitable sub-group of the compounds
for use in the compositions of this invention is that of the formula (II):
and pharmaceutically acceptable salts and in-vivo hydrolysable esters thereof, wherein
R
2, R
3 and R are as hereinbefore defined.
[0020] Preferably in the compounds of the formula (II)
R3 and
R4 are both hydrogen atoms and R
2 is selected from hydrogen, bromine, fluorine, chlorine, C
1-6 alkyl nitro and amino. Most favourably R and R are both hydrogen and R
2 is hydrogen, methyl, bromine or amino.
[0021] Preferably also in the compounds of the formula (II) R
2 and R
3 are on any two adjacent carbon atoms and represent a buta-1,3-dienylene moiety, thus
forming a naphthyl group.
[0022] Suitably also in the compounds of the formula (II) R
2, R
3 and R are all methyl groups.
[0023] The compounds of the formulae (I) - (II) are suitably provided in the form of the
free acid. Alternatively the compounds of the formulae (I) - (II) are provided in
the form of a pharmaceutically acceptable salt.
[0024] Examples of pharmaceutically acceptable salts of the compounds of the formulae (I)
- (II) include the alkali metal salts such as sodium or potassium,alkaline earth metal
salts such as calcium or magnesium, and ammonium or substituted ammonium salts for
example those with lower alkylamines such as triethylamine, hydroxy- lower alkylamines
such as 2-hydroxyethylamine, bis-(2-hydroxyethyl)-amine, tris-(hydroxymethyl)amine
or tris-(2-hydroxyethyl)-amine, cycloalkylamines such as bicyclohexylamine, or with
procaine, dibenzylamine, N,N-dibenzylethylenediamine, 1-ephenamine, N-ethylpiperidine,
N-benzyl-P-phenethylamine, dehydroabietyl- amine or N,N'-bis-dehydroabietylethylenediamine.
[0025] Thus suitable salts of this invention include the sodium, potassium, calcium, magnesium
and ammonium salts, of these the sodium, potassium and calcium salts are favoured.
[0026] The compounds of the formulae (I) - (II) may be provided as in-vivo hydrolysable
esters. Such esters are those which hydrolyse in the human body to produce the parent
acid. Suitable in-vivo hydrolysable esters include those esters known to give in-vivo
hydrolysis in penicillins. Thus suitable esters include those of the formula (ii):
wherein R
1 is a hydrogen atom, or a methyl or phenyl group; R
2 is an alkyl group of 1 to 6 carbon atoms, a phenyl group, an alkyl group of 1 to
3 carbon atoms substituted by a phenyl group, an alkoxy group of 1 to 6 carbon atoms,
a phenoxy group, or an alkoxy group of 1 to 3 carbon atoms substituted by a phenyl
group; or R
1 is attached to R
2 to form a 1,2-diphenylene or 4,5-dimethoxy-1,2-diphenylene group.
[0027] Favourably R
1 is hydrogen.
[0028] When R
1 is hydrogen suitably R
2 is selected from methyl, ethyl, n-propyl, iso
-propyl, n-butyl, tert-butyl, phenyl, benzyl, methoxy, ethoxy, n-propyloxy and iso-
propyloxy. Preferably R
2 is tert-butyl.
[0029] Favourably R
1 and R
2 are joined so that the ester is a phthalidyl or 3,4-dimethoxyphthalidyl ester.
[0030] Of these esters those favoured as in-vivo hydrolysable esters are the acetoxymethyl,
acetoxyethyl, phthalidyl, ethoxycarbonyloxymethyl, a-ethoxycarbonyloxyethyl and pivaloyloxymethyl
esters.
[0031] The in-vivo hydrolysable nature of the ester may be confirmed by administration to
an animal such as a mouse or rat and determination of the presence of a compound of
the formula (I) or a salt thereof in the blood or urine of the animal. Alternatively
hydrolysis in human blood or serum may be determined.
[0032] It must be realised that salts of the compounds of the formulae (I) - (II) formed
with pharmaceutically unacceptable ions are useful as they may serve as intermediates
in the preparation of pharmaceutically acceptable salts by ion-exchange, or they may
be useful as intermediates in the preparation of in-vivo hydrolysable esters. An example
of such a salt is the lithium salt.
[0033] The compositions of the invention include those in a form adapted for oral, topical
or parenteral use and may be used for the treatment of the infection in mammals including
humans.
[0034] Suitable forms of the compositions of this invention include tablets, capsules, creams,
syrups, suspensions, solutions, reconstitutable powders and sterile forms suitable
for injection or infusion. Such compositions may contain conventional pharmaceutically
acceptable materials such as diluents, binders, colours, flavours, preservatives,
disintegrant and the like in accordance with conventional pharmaceutical practice
in the manner well understood by those skilled in the art of formulating antibiotics.
[0035] Injectable or infusable compositions of a compound of the invention are particularly
suitable as high blood levels of the compound can occur after administration by injection
or infusion. Thus, one preferred composition aspect of this invention comprises a
compound of the invention in sterile form and most suitably in sterile crystalline
form.
[0036] The injectable solution of the compound of this invention may be made up in a sterile
pyrogen-free liquid such as water, aqueous ethanol or the like.
[0037] This invention also provides the use of a penicillin or cephalosporin or pharmaceutically
acceptable salt or in-vivo hydrolysable ester thereof in composition with a compound
of the formula (I) or pharmaceutically acceptable salt or in-vivo hydrolysable ester
thereof, for preparing injectable aqueous solutions.
[0038] Such solutions may be prepared by dissolving the sterile compound of this invention
and the penicillin or cephalosporin in sterile water. Suitably this water is "Water
for Injection BP" or the equivalent and may contain electrolytes to render it isotonic.
[0039] A particularly suitable injectable aqueous solution of this invention is one which
contains not less than 15% w/w of the salt of the compound of the formula (I).
[0040] Unit dose compositions comprising a compound of this invention adapted for oral administration
form a further suitable composition aspect of this invention.
[0041] Orally administrable compositions are of use as a synergistically effective blood
level can be expected at high dose and at lower doses such compositions may be used
to treat infections localised in the gastrointestinal tract.
[0042] Unit dose compositions comprising a compound of this invention adapted for topical
administration are also presented by this invention. In this instance 'topical administration'
also includes local administration to internal surfaces of mammary glands of cattle,
for example during the treatment of mastitis by intramammary administration. Considerable
advantages accrue from the inclusion of a penicillin or cephalosporin since the resulting
composition shows enhanced effectiveness (synergy).
[0043] Suitable penicillins for inclusion in the compositions of this invention include
benzylpenicillin, phenoxymethylpenicillin, carbenicillin, azidocillin, propicillin,
ampicillin, amoxycillin, epicillin, ticarcillin, cyclacillin, pirbenicillin, azlocillin,
mezlocillin, celbenicillin and other known penicillins including pro-drugs therefore
such as their in-vivo hydrolysable esters such as the acetoxymethyl, pivaloyloxymethyl,
α-ethoxycarbonyloxyethyl or phthalidyl esters of ampicillin, benzylpenicillin or amoxycillin,
and aldehyde or ketone adducts of penicillins containing a 6-o(-aminoacetamide side
chain ( such as hetacillin, metampicillin and analogous derivatives of amoxycillin)
or α-esters of carbenicillin or ticarcillin such as their phenyl or indanyl α-esters.
[0044] Suitable cephalosporins for inclusion in the compositions of this invention include
cefatrizine, cephaloridine, cephalothin, cefazolin, cephalexin, cephacetrile, cephamandole
nafate, cephapirin, cepradine, 4-hydroxycephalexin, cefaprole, cephaloglycin, and
other known cephalosporins or pro-drugs thereof.
[0045] Such compounds are frequently used in the form of a salt for example the sodium,
potassium or calcium salt or a hydrate thereof,
[0046] Naturally if the penicillin or cephalosporin present in the composition is not suitable
for oral administration then the composition will be adapted for parenteral administration.
As previously indicated such injectable or infusable compositions can be particularly
apt.
[0047] Highly favoured penicillins for use in the compositions of this invention include
ampicillin, amoxycillin, carbenicillin and ticarcillin. Such penicillins may be used
as a pharmaceutically acceptable salt such as the sodium salt.
[0048] Alternatively the ampicillin or amoxycillin may be used in the form of fine particles
of the zwitterionic form (generally as ampicillin trihydrate or amoxycillin trihydrate)
for use in an injectable suspension, for .example, in the manner hereinbefore described
for a composition of this invention.
[0049] The preferred penicillin for use in the synergistic composition is amoxycillin, for
example as its sodium salt or trihydrate.
[0050] Particularly suitable cephalosporins for use in the compositions of this invention
include cephaloridine and cefazolin.
[0051] When present together with a cephalosporin or penicillin, the ratio of a compound
of the invention to the penicillin or cephalosporin agent may vary over a wide range
of ratios, such as from 10:1 to 1:10 for example about 3:1, 2:1, 1:1, 1:2, 1:3, 1:4,
1:5 or 1:6, (wt/wt, based on pure free antibiotic equivalent).
[0052] The total quantity of a compound of the formula (I) or its pharmaceutically acceptable
salt or in vivo hydrolysable ester in any unit dosage will normally be between 25
and 1000 mg and will usually be between 50 and 500 mg, for example about 62.5, 100,
125, 150, 200 or 250 mg.
[0053] Compositions of this invention may be used for the treatment of infections inter
alia, the respiratory tract, the urinary tract and soft tissues in humans and mastitis
in cattle.
[0054] Normally between 50 and 1000 mg of a synergist will be administered each day of treatment
but more usually as 2, 3 or 4 doses.
[0055] The penicillin or cephalosporin in the synergistic composition of this invention
will normally be present at approximately the amount at which it is conveniently used
which will usually be expected to be from about 62.5 to 1000 mg per dose, more-usually
about 125, 250 or 500 mg per dose.
[0056] One particularly favoured composition of this invention will contain from 150 to
1000 mg of amoxycillin as the trihydrate or sodium salt and from 25 to 500 mg of a
synergist.
[0057] Most suitably this form-of composition will contain a pharmaceutically acceptable
salt of the compound of the formula (I).
[0058] A further particularly favoured composition of this invention will contain from 150
to 1000 mg of ampicillin or a pro-drug therefor and from 25 to 500 mg of a synergist.
[0059] Most suitably this form of composition will contain ampicillin trihydrate, ampicillin
anhydrate, sodium ampicillin, hetacillin, pivampicillin hydrochloride bacampicillin
hydrochloride or talampicillin hydrochloride. Most suitably this form of the composition
will contain a compound of the formula (I) or its pharmaceutically acceptable salt.
[0060] Most suitably the preceding compositions will contain from 200 to 700 mg of the penicillin
component. Most suitably the preceding composition will comprise from 50 to 250 mg
of a compound of the formula (I).
[0061] Such compositions may be adapted for oral or parenteral use except when containing
an in vivo hydrolysable ester of ampicillin or amoxycillin in which case the compositions
will not be adapted for parenteral administration.
[0062] Another particularly favoured composition of this invention will contain from 200
to 2000 mg of carbenicillin, ticarcillin or a pro-drug therefor and from 50 to 500
mg of a synergist.
[0063] Suitably this form of composition will contain di-sodium carbenicillin. Suitably
this form of the composition will contain di-sodium ticarcillin.
[0064] More suitably this form of the composition will contain from 75 to 250 mg of a compound
of the formula (I) or pharmaceutically acceptable salt or in vivo hydrolysable ester
thereof preferably in crystalline form. Such compositions containing di-salts of carbenicillin
and ticarcillin will be adapted for parenteral administration.
[0065] The present invention also provides a method of treating bacterial infections in
humans or domestic mammals which comprises the administration of a composition of
this invention.
[0066] Commonly the infection treated will be due to a strain of Staphvlococcus aureus,
Escherichia coli or Proteus sp. The organisms named are readily treated by using a
synergistically effective amount of the synergist and a penicillin or cephalosporin.
The administration of the two components may take place separately but in general
we prefer to use a composition containing both the synergist and the penicillin or
cephalosporin.
[0067] The indications for treatment include respiratory tract and urinary tract infections
in humans and mastitis in cattle.
[0068] The present invention also provides the compounds of the formula (I) or pharmaceutically
acceptable salts or in vivo hydrolysable esters thereof with the proviso that when
n is 0, then R
1 is not methyl, benzyl, p-chlorobenzyl, phenyl or p-aminophenyl when the compounds
of this invention are in the form of a free acid or a pharmaceutically-acceptable
salt.
[0069] Suitable classes of groups and novel compounds of this invention are those described
above in relation to the compounds of the formula (I) and (II) for use in the compositions
of this invention.
[0070] The compounds of the formula (I) or salts or esters thereof may be prepared by the
reaction of a compound of the formula (III), or a derivative thereof which allows
acylation to take place:
wherein n is O or 2 and R
x is a hydrogen atom or a carboxy protecting group, with an O-sulphonating derivative
of a compound of the formula (IV):
wherein R
1 is as hereinbefore defined in relation to formula (I); and thereafter if desired,
a) cleaving the carboxy protecting group to form the free acid or salt thereof.
b) converting the free acid or salt into a pharmaceutically acceptable salt or in-vivo
hydrolysable ester,
c) converting the compound wherein n is O to the compound wherein n is 2.
[0071] Suitable O-phonating derivatives include R
1SO
2Cl, R
1SO
2Br and (R
1SO
2)
2O; of these the sulphonyl chloride is preferred.
[0072] Suitable groups R
x include the hydrogen atom, in-vivo hydrolysable esters as hereinbefore described,
and conventional protecting groups well-known to those skilled in the art of penicillin
chemistry. Such conventional protecting groups include salts and ester derivatives
of the carboxylic acid.
[0073] The derivative is preferably one which may readily be cleaved at a later stage of
the reaction. Suitable salts include sodium, potassium, dicyclohexylamine and tertiary
amine salts, such as those with tri-lower- alkylamines, N-ethylpiperidine, 2,6-lutidine,
pyridine, N-methylpyrrolidine, dimethylpiperazine. A preferred salt is with triethylamine.
[0074] Suitable ester-forming carboxyl-protecting groups are those which may be removed
under conventional conditions. Such groups for R
x include benzyl, p-methoxybenzyl, 2,4,6-trimethylbenzyl, 3,5-di-t-butyl-4-hydroxybenzyl,
benzoylmethyl, p-nitrobenzyl, 4-pyridylmethyl, 2,2,2-trichloroethyl, 2,2,2-tribromoethyl,
t-butyl, t-amyl, diphenylmethyl, triphenylmethyl, adamantyl, 2-benzyloxyphenyl, 4-methylthiophenyl,
tetrahydro- f
Uran;2-yl, tetrahydropyran-2-yl, pentachlorophenyl, p-toluenesulphonylethyl, methoxymethyl,
a silyl group such as trimethylsilyl, a stannyl or phosphorus- containing group, or
an oxime radical of formula -N=CHR
o where R is aryl or heterocyclic.
[0075] The carboxyl group may be regenerated from any of the above esters by usual methods
appropriate to the particular R
X group, or by enzymatically - catalysed hydrolysis, or by hydrogenation.
[0076] Suitably the reaction of a compound of the formula (III) with a compound of the formula
(IV) is performed in the presence of an organic or inorganic base. More suitably the
base is an organic amine such as a tri-C
1-6 alkylamine or pyridine. Preferably the base is triethylamine. Inorganic bases may
be used for example sodium hydroxide, potassium hydroxide or sodium hydride.
[0077] Suitably the reaction of an ester of a compound of the formula (III) and a compound
of the formula (IV) as hereinbefore described is performed in an inert organic solvent,
for example diethylether, tetrahydrofuran, dioxan, 1,2-dimethoxyethane, chloroform,
dichloromethane, ethyl acetate, acetone and acetonitrile.
[0078] A particularly suitable solvent is dichloromethane.
[0079] The reaction of an inorganic salt of a compound of the formula (III) such as the
sodium or potassium salt and a compound of the formula (IV) is suitably performed
in an aqueous solvent system. The reaction of an organic amine salt of a compound
of the formula (III) and a compound of the formula (IV) is suitably performed in a
chlorinated solvent, for example dichloromethane.
[0080] Suitably the reaction is performed at a temperature between -30° and 30°. A particularly
preferred procedure is to commence the reaction at 0
0C and permit the reaction temperature to rise slowly to ambient.
[0081] Since it is frequently desirable to form a salt of the compound of the formula (I),
it is a preferred embodiment to use as the carboxyl protecting group in the compounds
of the formula (III) an ester that is readily converted to the parent acid or its
salt by mild methods of hydrogenolysis. Particularly suitable esters for use in this
process include benzyl esters optionally substituted by C
1-6 alkyl, C
1-6 alkoxy, bromine, chlorine or nitro. A preferred ester is the benzyl ester.
[0082] Suitable methods of hydrogenation include hydrogenation in the presence of a transition
metal catalyst. The pressure of hydrogen used in the reaction may be low, medium or
high but in general an approximately atmospheric or slightly super-atmospheric pressure
of hydrogen is preferred. The transition metal catalyst employed is preferably palladium
on charcoal or on calcium carbonate. The hydrogenation may be effected in any inert
solvent in which the ester is soluble for example tetrahydrofuran, ethyl acetate,
methanol, ethanol, and mixtures thereof together with water. If this hydrogenation
is carried out in the presence of a base then a salt of the compound of the formula
(I) is produced. Suitable bases for inclusion include NaHCO
3, KHCO
3, Na
2CO
3, CaCO
3, MgCO
3, LiHCO
3, NH
4OCOCH
3 and the like. If no base is present then hydrogenation leads to the preparation of
an acid within formula (I) which may then be neutralised if desired to yield a salt.
Suitable bases which may be used to neutralise acids within formula (I) include LiOH,
NaOH, NaHCO
3, KOH, Ca(OH)
2 and Ba(
OH)
2.
[0083] The salts of acids (I) may be converted to esters in conventional manner, for example
by reaction with a reactive halide such as bromomethyloxy pivalate in solution in
dimethylformamide.
[0084] The substituent group or groups within the groups R
2 and R
3 in the compounds of formula (I) may be varied by conventional reactions. Thus for
example when a substituent is a nitro group it may be reduced in a conventional manner
to an amino group, for example by catalysed hydrogenation. Similarly an amino group
may be acylated to give a substituted amino group, for example by treatment with an
acyl halide in the presence of an organic base. Substituents such as NHCO
2p-nitrobenzyl of OCO
2p-nitrobenzyl may be converted to an amino or hydroxyl group respectively for example
by hydrogenolysis.
[0085] The compounds of the formula (III) and derivatives thereof wherein n is 0 are described
in United States Patent No 4,143,046 which is herein incorporated by reference.
[0086] The compounds of formula (I) wherein n is 2, and pharmaceutically acceptable salts
and in-vivo hydrolysable esters thereof may be prepared by treatment of the corresponding
compound of the formula (I) wherein n is 0 with an oxidising agent in an inert solvent
at a non- extreme temperature, for example 0° - 30 C.
[0087] A suitable oxidising agent is m-chloroperbenzoic acid.
[0088] When the oxidising agent used is m-chloroperbenzoic acid suitable solvents include
water, diethyl ether, tetrahydrofuran, dioxan, ethyl acetate, chloroform and dichloromethane.
Preferred solvents are dichloromethane, diethyl ether and chloroform.
[0089] In analogous manner the compounds of the formula (III) wherein n is 2 may be prepared
from compounds of the formula (III) wherein n is 0.
[0090] The following Examples illustrate the invention.
Example 1
Calcium 6β-p-bromobenzenzsulphonyloxypenicillanate
[0091] Benzyl 6β-hydroxypenicillanate (0.202 g) was dissolved in chloroform (3 ml) containing
dimethylformamide (0.15 ml), and to this stirred solution was added p-bromobenzenesulphonyl
chloride (0.255 g) and triethylamine (0.092 ml). After 24 hours the reaction mixture
was diluted with chloroform (20 ml), washed with dilute sodium bicarbonate (15 ml),
washed with water (15 ml), dried (MgSO
4), and evaporated in vacuo to afford a gum. This gum was subjected to rapid column
chromatography on silica gel (20 g) using ethyl acetate:cyclohexane (1:3). The appropriate
fractions were combined and evaporated in vacuo to afford an oil, which was crystallised
from ethyl acetate-cyclohexane to yield benzyl 6β-p-bromobenzenz sulphonyloxy- penicillanate
as white crystals, m.p. 117-118°C; i.r. (Nujol)1795, 1755, 1745 cm
-1; n.m.r. (CDCl
3) 1.36(3H, s), 1.56(3H, s), 4.45(1H, s), 5.15(2H, s), 5.47(1H, d J =4Hz), 5.65(1H,
d J=4Hz), 7.35(5H, s), 7.77(4H, ABq J =9Hz).
[0092] Benzyl 6β-p-bromobenzenesulphonyloxypenicillanate (0.097 g) was dissolved in a solvent
mixture of tetrahydrofuran (3 ml), methanol (3 ml), and water (3 ml), and was hydrogenated
over 5% Palladium on calcium carbonate (0.3 g) for 1 hour. The catalyst was filtered
off and washed liberally with water and methanol. The combined filtrates were concentrated
in vacuo to afford the title compound as a white solid (0.09 g), i.r. (KBr) 3400,
1778, 1595 cm
-1; n.m.r.(D
20) 1.38(3H, s), 1.49(3H, s), 4.19(1H, s), 5.37 (1H, d J=4.5Hz), 5.87(1H, d J=4.5Hz),
7.5-8.1(4H, m).
Example 2
Sodium 6β-ethanesulphonyloxypenicillanate
[0093] To a solution of benzyl 6β-hydroxypenicillanate (0.5 g) in dichloromethane (10 ml)
containing triethylamine (0.4 ml) at -10°C was added ethanesulphonyl chloride (0.2
ml). The solution was stirred at -10°C for 15 min., then washed with iced water, dilute
hydrochloric acid, sodium bicarbonate, brine and finally dried over anhydrous magnesium
sulphate. Removal of the solvent in vacuo yielded benzyl 6β-ethanesulphonyloxypenicillanate
as a pale yellow oil (0.57 g),
v max (CHC1
3) 1800, 1750, 1500, 1460,
1370,
1300,
1280, 1180, 850 and 840 cm
-1;
+ 173.3° (c 1.2% CHCl
3), δ (CDCl
3) 7.35 (5H, s, ArH), 5.75 (1H, d, J = 3.7Hz, H-C
6), 5.52 (1H, d, J = 3.7Hz, H-C
5), 5.17 (2H, s, CH
2-Ph), 4.50 (1H, s, H-C
3), 3.28 (2H, q, J = 7.4Hz, Me-CH
2-S), 1.63 (3H, s, gem CH
3), 1.46 (3H, t, J - 7.4Hz, CH
3-CH
2-S), 1.43 (3H, s, gem CH
3)
[0094] Benzyl 6β-ethanesulphonyloxypenicillanate (0.2 g) was dissolved in tetrahydrofuran
(10 ml) containing water (3 drops) and 10% palladium-carbon catalyst (0.4 g). The
mixture was hydrogenolysed at atmospheric pressure for ½ hr, then filtered (celite)
and evaporated in vacuo. The resulting oil was partitionec between ethyl acetate:
water and neutralised with sodium hydroxide (0.5 M). The aqueous layer was separated
and the water removed in vacuo to yield sodium 6p-ethanesulphonyloxypenicillanate
as a pale brown solid (0.108 g), ν
max (KBr) 1750, 1610, 1520, 1430, 1360, 1240,
1170,
890 and 860 cm
-1;
= +219.4° (c 1.2 H20), δ (D
20) 5.92 (1H, d, J = 3.7 Hz, H-C
6), 5.61 (1H, d, J = 3.7Hz, H-C
5), 4.27 (1H, s, H-C
3), 3.46 (2H, q, Me-CH
2-S), 1.56 (3H, s, gem CH
3), 1.45 (3H, s, gem CH
3), 1.35 (3H, t, CH
3-CH
2-S).
Example 3
Sodium 6β-(2-naphthalene sulphonyloxy)penicillanate
[0095] To a solution of benzyl 6β-hydroxypenicillanate (0.6 g) in pyridine (10 ml) was added
2-naphthalenesulphonyl chloride (0.8 g). The solution was allowed to stand at 4°C
for 24 hr., and then poured on to iced water, and extracted with ethyl acetate (2
x 20 ml). The ethyl acetate layer was then washed with dilute sulphuric acid (2 x
40 ml) and dried over anhydrous sodium sulphate - sodium carbonate. Removal of the
solvent in vacuo yielded benzyl 6β-(2-naphthalenesulphonyloxy)penicillanate as a pale
yellow oil (0.5 g), ν
max (CHC13) 1800, 1750, 1460, 1180, and 900 cm
-1; δ (CDCl
3) 7.55 (7H, m, ArH), 7.35 (5H, s, ArH ester), 5.70 (lH, d, J = 4Hz, H-C
6), 5.45 (1H, d, J = 4Hz, H-C
5), 5.15 (2
H, s, CH
2-Ph), 4.45 (1H, s, H-C
3), 1.55 (3H, s, gem CH
3), 1.35 (3H, s, gem
CH
3).
[0096] Benzyl 6β-(2-naphthalenesulphonyloxy)penicillanate (0.4 g) was dissolved in tetrahydrofuran
(15 ml) containing water (3 drops) and 10% palladium - carbon catalyst (0.8 g). The
mixture was hydrogenolysed at atmospheric pressure for ½ hr, then filtered (celite)
and the solvent evaporated in vacuo. The resulting oil was partitioned between ethyl
acetate : water and neutralised with sodium hydroxide (0.5 M). The aqueous layer was
separated and freeze dried to yield sodium 6β-(2-naphthalenesulphonyloxy)-penicillanate
as a white solid, ν
max (KBr), 1785, 1610, 1410, 1390, 1230, 1185 and 900 cm
-1; δ (D
20) 8.65 (1H, s, ArH), 8.00 (6H, m, ArH), 6.05 (1H, d, J = 3.8Hz, H-C
6), 5.55 (lH, d, J = 3.8Hz, H-C
5), 4.23 (1H, s, H-C
3), 1.60 (3H, s, gem CH
3), 1.50 (3H, s, gem C
H3).
Example 4
Sodium 6β-mesitylenesulphonyloxypenicillanate
[0097] To a solution of benzyl 6β-hydroxypenicillanate (0.64 g) in pyridine (10 ml) was
added mesitylenesulphonyl chloride (0.5 g) The solution was allowed to stand at 4°C
for 24 hr. then poured on to iced water and extracted with ethyl acetate (2 x 20 ml).
The ethyl acetate layer was then washed with dilute sulphuric acid (2 x 20 ml) and
dried over anhydrous sodium sulphate - sodium carbonate. Removal of the solvent in
vacuo yielded benzyl 6β-mesitylenesulphonyloxypenicillanate (0.8 g), v
max (CHCl
3) 1790, 1740, 1600, 1190 and 880 cm
-1; δ (d
6-DMSO) 7.40 (5H, s, ArH), 7.15 (2H, s, ArH), 5.85 (1H, d, J = 3.8Hz, H-C
6), 5.48 (1H, d, J = 3.8Hz, H-C
5), 5.20 (2H, s, CH
2Ph), 4.55 (1H, s, H-C
3), 2.60 (6H, s, ArCH
3), 2.30 (3H, s, ArCH
3), 1.55 (3H, s. gem CH
3), 1.35 (3H, s, gem CH
3).
[0098] Benzyl 6β-mesitylenesulphonyloxypenicillanate (0.45 g) was dissolved in tetrahydrofuran
(15 ml) containing water (3 drops) and 10% palladium-carbon catalyst (0.9 g). The
mixture was hydrogenolysed at atmospheric pressure for ½ hr. then filtered (celite)
and the solvent evaporated in vacuo. The resulting oil was partitioned between ethyl
acetate : water and neutralised with sodium hydroxide (0.5 M). The aqueous layer was
separated and freeze dried to yield sodium 6β-mesitylenesulphonyloxypenicillanate
as a white solid (0.39 g), v
max (KBr), 1780, 1600, 1190 and 850 cm ; δ (D
2O) 6.90 (2H, s, ArH), 5.62 (1H, d, J = 3.8Hz, H-C
6), 5.30 (1H, d, J = 3.8Hz, H-C
5), 4.05 (1H, s, H-C
3), 2.35 (6H, s, ArCH
3), 2.05 (3H, s, ArCH
3), 1.35 (3H, s, gem CH
3), 1.25 (3H, s, ge
m CH
3),
Example 5
Sodium 6β-(p-bromobenzenesulphonyloxy)penicillanate
[0099] To a solution of benzyl 6β-hydroxypenicillanate (1.2 g) in pyridine (20 ml) was added
p-bromobenzenesulphonyl chloride (2 g). The solution was allowed to stand at 4°C for
24 hr. then poured on to iced water and extracted with ethyl acetate (2 x 20 ml).
The ethyl acetate layer was then washed with dilute sulphuric acid (2 x 100 ml) and
dried over anhydrous sodium sulphate - sodium carbonate. Removal of the solvent in
vacuo yielded benzyl 6β-(p-bromobenzenesulphonyloxy)penicillanate as an orange brown
solid which was purified by reprecipitation from ethyl acetate at -70°C by the addition
of light petrol, to give an off white solid (1.6 g).
[0100] Benzyl 6β-(p-bromobenzenesulphonyloxy)penicillanate (0.6 g) was dissolved in tetrahydrofuran
(15 ml) containing water (3 drops) and 10% palladium-carbon catalyst (1.2 g). The
mixture was hydrogenolysed at atmospheric pressure for ½ hr then filtered (celite)
and the solvent removed. The resulting oil was partitioned between ethyl acetate :
water and neutralised with sodium hydroxide (0.5 M). The aqueous layer was separated
and the water removed under reduced pressure to yield a pale brown solid (0.36 g),
v
max (KBr) 1775, 1610, 1090 and 890 cm
-1; δ (D
20) 7.80 (4H, m, ArH) 5.90 (1H, d, J = 4Hz, H-C
6), 5.40 (1
H, d, J = 4Hz, H-C
5), 4.19 (1H, s, H-C
3), 1.55 (3H, s, gem CH
3), 1.40 (3H, s, gem CH
3).
Example 6
Sodium 6β-(p-toluenesulphonyloxy)penicillanate 1,1-dioxide
[0101] To a solution of benzyl 6β-hydroxypenicillanate 1,1-dioxide (0.5 g) in pyridine (15
ml) at 0°C was added p-toluenesulphonyl chloride (0.6 g). The solution was allowed
to stand at 4°C for 24 hr then poured on to iced water and extracted with ethyl acetate
(2 x 20 ml). The ethyl acetate layer was washed with dilute sulphuric acid (2 x 30
ml) and finally dried over sodium sulphate - sodium carbonate. Removal of the solvent
in vacuo yielded benzyl 6β-(p-toluenesulphonyloxy)penicillanate 1,1-dioxide as a pale
yellow oil (0.58 g), ν
max (CHC1
3), 1820, 1750, 1600 cm
-1; δ (CDCl
3) 7.88 (2H, m, ArH), 7.35 (7H, m, ArH), 5.80 (1H, d, J = 4Hz, H-C
6), 5.20 (2H, q, CH
2-Ph), 4.75 (1H, d, J = 4Hz, H-C
5), 4.50 (1H, s, H-C
3 2.44 (3H, s, ArCH
3), 1.23 (3H, s, gem CH
3).
[0102] Benzyl 6β-(p-toluenesulphonyloxy)penicillanate 1,1-dioxide (0.2 g) was dissolved
in terrahydrofuran(10ml) containing water (3 drops) and 10% palladium-carbon catalyst
(0.4 g). The mixture was hydrogenolysed at atmospheric pressure for ½ hr then filtered
(celite). Removal of the solvent in vacuo from the filtrate yielded a colourless glass
which was dissolved in ethyl acetate (1 ml) to which solution 2M sodium 2-ethyl hexanoate
in methyl isobutyl ketone (0.13 ml) was addded. Sodium 6β-(p-toluene- sulphonyloxy)penicillanate
1,1-dioxide was precipitated from the solution by addition of diethyl ether (20ml),
as a white solid (0.14 g), ν
max(KBr), 1800, 1620, 1460 and 1180 cm
-1; δ (D
20) 7.60 (4H, m, ArH), 6.03 (1H, d, J = 4Hz, H-C
6), 5.10 (1H, d, J = 4Hz, H-C
5), 4.32 (1H, s, H-C
3), 2.39 (3H, s, ArCH
3), 1.50 (3H, s, gem CH
3), 1.35 (3H, s, gem C
H3).
Example 7
Lithium 6β-(p-toluenesulphonyloxy)penicillanate
[0103] Benzyl 6β-hydroxypenicillanate (0.202g) was dissolved in chloroform (4ml) containing
dimethylformamide (0.15 ml). To this stirred solution at 0°C was added p-toluenesulphonyl
chloride (0.087 g) and triethylamine (0.092 ml). The reaction mixture was allowed
to warm to room temperature. After 48 hours, the reaction mixture was diluted with
chloroform (20 ml), washed with dilute sodium bicarbonate (20 ml), washed with water
(20 ml), dried (MgSO
4), and evaporated in vacuo to afford an oil. This oil was subjected to column chromatography
on silica gel (20 g) using ethyl acetate:cyclohexane (1:3). The appropriate fractions
were combined and evaporated in vacuo to afford the title compound as a gum, which
was crystallised from ethyl acetate-cyclohexane to yield benzyl 6β-(p-toluenesulphonyloxy)
penicillanate as white crystals (0.09 g) m.p. 97°C; i.r. (Nujol) 1790, 1757 cm
-1; n.m.r. (CDC1
3) 1.37(3H, s), 1.57(3H, s), 2.45(3H, s), 4.46(lH, s), 5.16(2H, s), 5.45(lH, d J=4Hz),
5.62(1H, d J=4Hz), 7.35(5H, s), 7.60(4H, ABq J=9H
2).
[0104] Benzyl 6β-(p-toluenesulphonyloxy)penicillanate (0.078 g) in tetrahydrofuran (15 ml)
was hydrogenated over 10% palladium-carbon catalyst (0.12 g) for 4 hr. The mixture
was then filtered (celite), evaporated to 1 ml and water (5 ml) added. The resulting
solution was titrated to pH 7.0 with LiOH and the solvent removed to yield, after
washing with ether, lithium 6β-(p-toluenesulphonyl
oxy)penicillanate as a pinkish white solid (0.055 g), ν
max (KBr), 1780, 1610, 1195, 1180 cm
-1; (D
20) 7.75 (2H, d, J = 8Hz, ArH), 7.34 (2H, d, J = 8Hz, ArH), 5.84 (1H, d, J = 3Hz, H-C
6), 5.37
(lH,
d,
J = 3Hz,
H-C5),
4.
19 (1H,
s, H-C
3),
2.32 (3H, s, ArH), 1.49 (3H, s, gem CH
3), 1.39 (3H, s, gem CH
3).
Example
Sodium 6β-(p-nitrobenzenesulphonyloxy)penicillanate
[0105] To a solution of sodium 6β-hydroxypenicillanate (0.78 g) in dimethylformamide was
added methoxymethyl chloride (0.65 ml). The solution was stirred at 0°C for 15 min
then poured on to iced water and extracted with ethyl acetate (3 x 30 ml). The ethyl
acetate layer was separated, washed with water, dried over anhydrous magnesium sulphate,
and the solvent removed in vacuo. The resulting oil was chromatographed on silica
gel (ethylacetate : petrol) to yield methoxymethyl 6β-hydroxypenicillanate (0.51 g),
ν
max (CHCl
3) 1790, 1760, 1400, 1160 cm
-1, δ (CDC1
3) 5.58 (1H, d, J = 4Hz,H-C
6), 5.13 (1H, d, J = 4 Hz, H-C
5), 5.30 (2H, s, CH
2O), 3.49 (3H, s, CH
3O), 1.67 (3H, s, gem CH
3), 1.55 (3H, s, gem CH
3).
[0106] Methoxymethyl 6β-hydroxypenicillanate (0.46 g) was dissolved in pyridine (2 ml) and
p-nitrobenzenesulphonylchloride (0.4 g) added. The solution was allowed to stand at
4°C for 24 hr., then poured onto iced water and extracted with ethyl acetate(2 x 20
ml). The ethyl acetate layer was separated, washed with dilute sulphuric acid (2 x
40 ml) and dried over anhydrous sodium sulphate-sodium carbonate. Removal of the solvent
in vacuo yielded methoxymethyl 6β-(p-nitrobenzenesulphonyloxy)penicillanate (0.7 g)
as a pale brown oil, ν
max (CHCl
3) 1800, 1750, 1540, 1350, 1190 cm
-1; δ (CDC13) 8.43 (2H, d, J = 9 Hz, ArH), 8.13 (2H, d, J = 9 Hz, ArH), 5.78 (lH, d,
J = 4 Hz, H-C
6), 5.53 (1H, d, J = 4 Hz, H-C
5), 5.28 (2H, s, CH
2O), 4.45 (lH, s, H-C
3), 3.45 (3H, s, OCH
3), 1.60 (3H, s, gem CH
3), 1.50 (3H, s, gem CH
3).
[0107] To a solution of methoxymethyl 6β-(p-nitrobenzenesulphonyloxy)-
penicillanate (0.18 g) in dimethylformamide was added lithium bromide (0.3
g). The solution was stirred overnight, then poured onto iced water and extracted with
ethyl acetate (3 x 30 ml). Theethyl acetate layer was separated, washed with water
and dried over anhydrous magnesium sulphate. The solution was then reduced to a small
volume (5 ml), water (5 ml) was added and the pH was adjusted to 7.5 with sodium hydroxide.
The aqueous layer was separated and the water removed in vacuo to yield a pale yellow
glass (0.13 g) which on silica gel chromatography using butanol : ethanol : water
(4:1:1)as eluant yielded sodium 6β-(p-nitrobenzenesulphonyloxy)-penicillanate (0.07
g) as a pale yellow glass, ν
max (KBr) 1780, 1605, 1535, 1350, 1190 cm
-1; δ (D
20) 8.34 (2H, d, J = 9 Hz, ArH), 8.05 (2H, d, J = 9 Hz, ArH), 5.88 (1H, d, J = 4 Hz,
H-C
6), 5.43 (1H, d, J = 4 Hz, H-C
5), 4.16 (1H, s, H-C
3), 1.43 (3H, s, gem CH
3), 1.35 (3H, s, gem CH
3).
Example
Composition
[0108]
a) A solution for injection may be prepared by dissolving 100 mg of sterile sodium
6β-methanesulphonyloxypenicillanate and 250 mg of sterile sodium amoxycillin in 1
ml of sterile water.
b) A solution for injection may be prepared by dissolving 125 mg of sterile sodium
6β-methanesulphonyloxypenicillanate and 125 mg of sterile cephaloridine in 1.5 ml
of sterile water.
Demonstration 1
Sodium 6β-methanesulphonyloxypenicillanate
[0109] Benzyl 6β-hydroxypenicillanate (0.202 g) was dissolved in chloroform (4 ml) containing
dimethylformamide (0.15 ml). To this stirred solution at 0°C, was added methanesulphonyl
chloride (0.052 ml) and triethylamine (0.092 ml). The reaction mixture was allowed
to warm to room temperature. After 20 hours, the reaction mixture was diluted with
chloroform (20 ml), washed with dilute sodium bicarbonate (20 ml), washed with water
(20 ml), dried (MgSO
4), and evaporated in vacuo to afford an oil. This oil was subjected to column chromatography
on silica gel (25 g) using ethyl acetate:cyclohexane (1:3). The appropriate fractions
were combined and evaporated in vacuo to afford benzyl 6p-methanesulphonyloxypenicillanate
as an oil (
0.
11 g); i.r. (liq film) 1795, 1740 cm
-1; n.m.r.(CDCl
3) 1.41(3H, s), 1.64(3H, s), 3.18(3H, s), 4.51(1H, s), 5.19 (2H, s), 5.57(1H, d J=4Hz),
5.76(1H, d J=4 Hz), 7.36(5H, s).
[0110] Benzyl 6β-methanesulphonyloxypenicillanate (0.10 g) was dissolved in a solvent mixture
of tetrahydrofuran (3 ml), methanol (3 ml), and water (3 ml), and was hydrogenated
over 5% Palladium on calcium carbonate (0.25 g) for 3 hours. The catalyst was filtered
off and washed liberally with water and methanol. The combined filtrates were concentrated
in vacuo to approximately 20 ml, and passed through an Amberlite IR-120(Na⊖) ion-exchange
column. The eluent was co-evaporated with n-propanol to afford the title compound
as a white solid (0.065 g), i.r.(KBr) 3400 (broad), 1785, 1740 sh, 1650 sh, 1605 cm
-1 ; n.m.r.(D20) 1.48(3H, s), 1.57(3H, s), 3.30(3H, s), 4.29(1H, s), 5.52(lH, d J=4Hz),
5.98(lH, d J=4Hz).
Demonstration 2 :
Sodium 6β-methanesulphonyloxypenicillanate
[0111] To a solution of benzyl 6β-hydroxypenicillanate (1.8 g) in dichloromethane (10 ml)
containing triethylamine (1.5 ml) at -10° was added methanesulphonyl chloride (1.0
ml). The solution was stirred at -10°C for 15 min, then washed with iced water, silute
hydrochloric acid, sodium bicarbonate, brine and finally dried over anhydrous magnesium
sulphate. Removal of the solvent in vacuo yielded benzyl 6β-methanesulphonyloxypenicillanate
as a pale yellow oil (2.1 g).
[0112] Benzyl 6β-methanesulphonyloxypenicillanate (2.0 g) was dissolved in tetrahydrofuran
(50 ml) containing water (3 drops) and 10% palladium-carbon catalyst (4 g). The mixture
was hydrogenolysed at atmospheric pressure for ½ hr then filtered (celite) and the
solvent evaporated in vacuo. The resulting oil was partitioned between ethyl acetate:
water and neutralised with sodium hydroxide (0.5 M). The aqueous layer was separated
and freeze dried to afford sodium 6β-methanesulphonyloxypeniciilanate as an off-white
solid (1.2 g).
Demonstration 3
Sodium 6β-phenylmethanesulphonyloxypenicillanate
[0113] To a solution of benzyl 6β-hydroxypenicillanate (0.5 g) in dichloromethane ( 10 ml)
containing triethylamine (0.4 ml) at -10°C was added phenylmethanesulphonyl chloride
(0.3 g). The solution was stirred at -10°C for 15 min., then washed with iced water,
dilute hydrochloric acid, sodium bicarbonate, brine and finally dried over anhydrous
magnesium sulphate. Removal of the solvent in vacuo yielded benzyl 6β-phenylmethanesulphonyloxy-
penicillanate as a pale yellow oil (0.61
g), v
max (CHCl
3), 1790, 1740, 1380, 1190, 890 and 840 cm
-1; δ (CDC13 7.41 (10H,
m, ArH),
5.52 (1H, d, J
= 4Hz, H-C
6), 5.37 (1H, d, J = 4Hz, H-C
5), 5.18 (2H, s, Ph-CH
2-S), 4.53 (3H, s, Ph-CH
2-O, and H-C
3), 1.60 (3H, s, gem CH
3), 1.43 (3H, s, gem CH
3).
[0114] Benzyl 6β-phenylmethanesulphonyloxypenicillanate (0.4 g) was dissolved in tetrahydrofuran
(25 ml) containing 10% palladium-carbon catalyst (0.8 g) and water (3 drops). The
mixture was hydrogenolysed at atmospheric pressure, for ½ hr. then filtered (celite)
and the solvent evaporated in vacuo. The resulting oil was partitioned between ethyl
acetate : water and neutralised with sodium hydroxide (0.5 M). The aqueous layer was
separated and the water removed in vacuo to yield sodium 6β-phenylmethanesulphonyloxy-
penicillanate as a white solid (0.3 g), ν
max (KBr) 1775, 1350, 1200, 1175, 890 and 840 cm
-1; δ (D
20) 7.49 (5H, s, ArH), 5.75 (1H, d, J = 4Hz, H-C
6), 5.45 (lH, d, J = 4Hz, H-C
5), 4.82 (2H, s, CH
2-Ph), 4.25 (1H, s, H-C
3), 1.55 (3H, s, gem CH
3), 1.45 (3H, s, gem CH
3),
= +167.8
0 (c 1.1 H
20).
Demonstration 4
Sodium 6β-benzenesulphonyloxypenicillanate
[0115] To a solution of benzyl 6β-hydroxypenicillanate (1.0 g) in pyridine (20 ml) was added
benzenesulphonyl chloride (0.5 ml). The solution was allowed to stand at 4°C for 24
hr then poured onto iced water and extracted with ethyl acetate (2 x 40 ml). The ethyl
acetate layer was then washed with dilute sulphuric acid (2 x 40 ml) and dried over
anhydrous sodium sulphate-sodium carbonate. Removal of the solvent in vacuo yielded
benzyl 6β-benzenesulphonyloxypenicillanate as a pale yellow oil (1.04
g), ν
max (CHCl
3) 1790, 1740, 1190 cm
-1; δ (CDCl
3) 7.83 (5H, m, ArH), 7.35 (5H, s, ArH ester), 5.65 (lH, d, J=3.5 Hz, H-C
6), 5.45 (1H, d, J=3.5 Hz, H-C
5), 5.18 (2H, s, CH
2-Ph), 4.47 (1H, s, H-C
3), 1.56 (3H, s, gem CH
3), 1.38 (3H, s, gem CH
3).
[0116] Benzyl 6β-benzenesulphonyloxypenicillanate (1.1 g) was dissolved in aqueous tetrahydrofuran
(10%, 30 ml), containing 10% palladium-carbon catalyst (2.3 g). The mixture was hydrogenolysed
for ½ hr at atmospheric pressure then filtered (celite) and the solvent removed in
vacuo to yield 6β-benzenesulphonyloxy- penicillanic acid (0.8 g) as a pale yellow
oil. The oil was dissolved in ethyl acetate (5 ml) and 2M sodium 2-ethyl hexanoate
in methyl isobutyl ketone (1 ml) was added. 6β-benzene- sulphonyloxypenicillanic acid
was precipitated as the sodium salt (on the addition of diethyl ether (50 ml)) in
the form of a red brown solid which crystallised on addition of water as colourless
needles, ν
max (KBr), 1790,-1600, 1190 and 855 cm
-1; δ (d
6-DMSO) 7.85 (5H, m, ArH), 5.97 (1H, d, J = 3.5 Hz, H-C
6), 5.33 (1H, d, J = 3.5 Hz, H-C
5), 4.18 (1H, s, H-C
3), 1.45 (3H, s, gem CH
3), 1.40 (3H, s, gem CH
3),
= +157.3° (c. 0.6
7 H20).
Demonstration 5
Sodium 6β-(p-aminobenzenesulphonyloxy)penicillanate
[0117] To a solution of benzyl 6β-hydroxypenicillanate (0.5 g) in pyridine (10 ml) was added
p-nitrobenzenesulphonyl chloride (0.6 g). The solution was allowed to stand for 24
hr. at 4°C, then poured onto iced water and extracted with ethyl acetate (2 x 20 ml).
The ethyl acetate layer was washed with dilute sulphuric acid (2 x 40 ml) and dried
over anhydrous sodium sulphate-sodium carbonate. Removal of the solvent yielded benzyl
6β-(p-nitrobenzenesulphonyloxy)-penicillanate as a pale yellow solid (0.5 g), v
max (CHCl
3) 1800, 1740, 1600, 1530, 1190 cm
-1 δ (CDC1
3) 8.40 (2H, d, J = 9 Hz, ArH), 8.13 (2H, d, J = 9 Hz, ArH), 7.35 (5H, s, CH
2-Ph), 5.75 (1H, d, J = 4 Hz, H-C
6), 5.52 (1H, d, J = 4 Hz, H-C
5), 5.16 (2H, s, CH
2-Ph), 4.47 (1H, s, H-C
3), 1.53 (3H, s, gem CH
3), 1.36 (3H, s, gem CH
3).
[0118] Benzyl 6β-(p-nitrobenzenesulphonyloxy)penicillanate (0.37) was dissolved in aqueous
tetrahydrofuran (20 ml) containing 10% palladium-carbon catalyst (0.7 g). The mixture
was hydrogenolysed at atmospheric pressure, until hydrogen uptake ceased, then filtered
(celite) and removed in vacuo. The resulting oil was partitioned between ethyl acetate:
water and neutralised with sodium hydroxide (0.5M). The aqueous layer was separated
and the water removed in vacuo to yield a pale yellow-glass which after silica gel
chromatography (butanol:ethanol:water) (4:1:1) yielded sodium 6β-(p-aminobenzene-
sulphonyloxy)penicillanate as an off-white solid (0.1 g), v
max (KBr) 1775, 1660, 1595, 1500, 1200, 1170 cm
-1; δ (D
20) 7.63 (2H, d, J = 9 Hz, ArH), 6.76 (2H, d, J = 9 Hz, ArH), 5.74 (1H, d, J = 4 Hz,
H-C
6), 5.32 (1H, d, J = 4 Hz, H-C
5), 4.15 (1H, s, H-C
3), 1.47 (3H, s, gem CH
3), 1.35 (3H, s, gem CH
3).
Demonstration of effectiveness
[0119] In standard MIC tests the activities of the compounds of Example 1 and Demonstration
1 alone, and in combination with ampicillin were determined against Staph Russell
and Proteus C889.
[0120] A composition of sodium 6β-methanesulphonyloxypenicillanate and cephaloridine against
7 cephalosporinase - producing E. coli strains results in the following MIC's in a
standard test.